Pediatric Klippel-Feil Syndrome

Klippel-Feil syndrome is a genetic (present at birth) condition where two or more cervical vertebrae (spinal bones of the neck) are fused.

What is Pediatric Klippel-Feil Syndrome?

The fused vertebrae that occur due to Klippel-Feil syndrome cause three distinguishing features, including a limited range of motion, low hairline at the back of the head and a short neck. Children with Klippel-Feil syndrome typically have one or two of the features, but some can have all three.

What are the causes of Pediatric Klippel-Feil Syndrome?

The cervical vertebrae fuse during the child’s development in their mother’s womb. The exact cause is unknown.